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MR Spectroscopy as a Diagnostic and Outcome Measure in Pain and SCI

CompletedNCT00561782
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The goal of this study is to compare the changes that occur in sensation and chemical properties of the brain following SCI between individuals that experience chronic pain and those that do not, and between those with SCI and the able-bodied.

Study details

Official title
MR Spectroscopy (MRS) as a Diagnostic and Outcome Measure in Pain and SCI
Conditions
Sponsor
US Department of Veterans Affairs
Collaborators
University of Miami
Organization
VA Office of Research and Development
Start date
2007-10
Primary completion
2010-11
Sex
All
Age range
from 18 Years to 70 Years
Healthy volunteers
true
Results posted
No results posted in this snapshot
Countries
United States
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. SCI and neuropathic pain: * fluent in English * incomplete or complete traumatic SCI * the injury must have occurred at least 2 years prior to entering the study * the injury level must be above L1 and the subjects must have evidence of preserved distal cord functions (lower extremity reflexes and bulbocavernosus or anal wink reflexes) * must have experienced chronic neuropathic pain at or below the level of injury for a minimum of six months * must have moderately severe or greater neuropathic pain * must be able to attend three sessions ranging from 2 to 6 hours over a period of 4 to 5 weeks 2. SCI and no neuropathic pain: \- same as a., but participants in this group must NOT have unremitting moderate-severe pain and there will only be two sessions ranging from 2 to 6 hours over a period of 1 to 2 weeks 3. Able-bodied control subjects: * fluent in English * no history of chronic pain conditions * no substantial brain or body injury * must be able to attend two sessions ranging from 2 to 6 hours over a period of 1 to 2 weeks Exclusion Criteria: * current pregnancy or women who are contemplating pregnancy * recent (one-year) history of alcohol or drug abuse * known intra-cerebral pathology or epilepsy * MRI findings indicative of intra-cerebral pathology * significant post-traumatic encephalopathy from head trauma sustained at SCI or cognitive impairment indicative of traumatic brain injury * current diagnosis of DSM-IV Axis I disorder * inability to meet the MRI screening requirements (including, but not limited to, the presence of a pacemaker or other electronic devices, prosthesis, artificial limb or joint, shunt, some metal rods, some tattoos, or moderate to severe claustrophobia or anxiety)

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT00561782